A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv564385



Internal ID16351794
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr14:37777235..37852402hg38UCSC Ensembl
Innerchr14:38246440..38321607hg19UCSC Ensembl
Innerchr14:37316191..37391358hg18UCSC Ensembl
Cytoband14q21.1
Allele length
AssemblyAllele length
hg3875168
hg1975168
hg1875168
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv825980
Samples
Known Genes
MethodSNP array
AnalysisIllumina SNP array copy number analysis
PlatformNot reported
Comments
ReferenceCooper_et_al_2011
Pubmed ID21841781
Accession Number(s)nsv564385
Frequency
Sample Size17421
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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